Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletion
Published inEuropean journal of haematology, vol. 77, no. 2, p. 169-174
Publication date2006-08
Abstract
Keywords
- Acidosis / genetics
- Adolescent
- Anemia, Refractory / genetics
- Anemia, Sideroblastic / genetics
- Anemia, Sideroblastic / metabolism
- Bone Marrow / pathology
- Cytochrome-c Oxidase Deficiency / genetics
- DNA Mutational Analysis
- DNA, Mitochondrial / genetics
- Disease Progression
- Electron Transport
- Electron Transport Complex IV / analysis
- Electron Transport Complex IV / genetics
- Fatal Outcome
- Gene Deletion
- Heterozygote
- Humans
- Iron / metabolism
- Male
- Mitochondria / metabolism
- Mitochondrial Myopathies / blood
- Mitochondrial Myopathies / genetics
- Mitochondrial Proton-Translocating ATPases / deficiency
- Mitochondrial Proton-Translocating ATPases / genetics
- Mosaicism
- RNA, Transfer / genetics
- Beta-Thalassemia / genetics
Affiliation entities
Funding
- FNS - [3200B0-102039]
Citation (ISO format)
MATTHES, Thomas et al. Different pathophysiological mechanisms of intramitochondrial iron accumulation in acquired and congenital sideroblastic anemia caused by mitochondrial DNA deletion. In: European journal of haematology, 2006, vol. 77, n° 2, p. 169–174. doi: 10.1111/j.1600-0609.2006.00674.x
Main files (1)
Article (Published version)
Identifiers
- PID : unige:163819
- DOI : 10.1111/j.1600-0609.2006.00674.x
- PMID : 16856911
Journal ISSN0902-4441